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Pre-dose cells from customers (four responders and three non-responders to BRAFi monotherapy) were profiled for phosphotyrosine kinase (PTK) and serine-threoninrametinib showed an antagonism on the STK activities and a synergism on PTK activities, resulting in stronger inhibitions of overall tyrosine kinase activities. Completely ; these data reveal that opposition of tumours and cellular outlines to MAPK inhibitors are predicted using a multiplex kinase assay and it is associated with a r
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